Canonical Allele Identifier: CA2750127458
Gene: MIR4432HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.60381626G>C , CM000664.2:g.60381626G>C GRCh38
NC_000002.11:g.60608761G>C , CM000664.1:g.60608761G>C GRCh37
NC_000002.10:g.60462265G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_132991.1:n.93+1318C>G
NR_132992.1:n.70+9680C>G